Affordable Access

[Gorlin-Goltz phakomatosis (author's transl)].

Authors
Type
Published Article
Journal
Archives d'ophtalmologie
Publication Date
Volume
37
Issue
3
Pages
221–236
Identifiers
PMID: 142475
Source
Medline
License
Unknown

Abstract

Having had the occasion of observing a new case, the authors have started on a new description of a specific autosomal dominant inheritance disease, description which connects an eye trouble with basal cell nevi, with jaw cysts as well as with malformations of the skeleton and nervous lesions, the tumoral lesions having the essential characteristic of possessing and evolutive potential. The authors explain the reasons which have led them to give to this specific disease the name of Gorlin-Goltz phacomatosis.

Statistics

Seen <100 times